7 offerte di lavoro trovate per life sciences .

For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Scientist based in the canton of Fribourg.  Your Impact:Implement and optimize robust, compliant, and high-performing manufacturing processes aligned with quality strategyCapitalize on and share your expertise throughout the entire product lifecycleDraft, review, and approve key technical documents (batch records, procedures,

CQ EngineerFor our Client a biopharmaceutical company in the Aargau we are currently seeking a number of CQ engineers.The C & Q Execution Engineer is primarily responsible for the execution of the CQV activities corresponding to their project area’s equipment and processes. Key Responsibilities:System Boundary development + approvalDesign Qualification preparation, execution and approval. Includes release for IQ.Good Manufacturing Practice (GMP) Rapid

For our client based in Aubonne, we are currently looking for a Regulatory Compliance Specialist for a 12-month contract.Your role:As a Regulatory Compliance Specialist, you will ensure that local manufacturing activities and GMP documentation remain fully aligned with regulatory filings.You will assess and manage change controls, ensuring timely and accurate reporting to Health Authorities.You will review and approve GMP documents, ensuring compliance

For one of our clients, an international pharmaceutical company, we are seeking a Project Technical Lead (Automated Visual Inspection).General Information:Start date: ASAPDuration: until 28.02.2026Workplace: Opfikon, ZurichHome office: PossibleWorkload: 100%Working hours: StandardTasks & Responsibilities:Develop URS and TechSpecs for AVI in IV bag applicationsLead the end-to-end process of identifying, evaluating, and conceptualizing Automated Visual

For our Client in Visp we are searching for a Technical Document Manager who is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases.  Key Responsibilities: Responsible for performance qualification (PQ) from detailed design through execution. This includes both CapEx-driven mechanical adaptations managed by external engineering (EPCM) partner and OpEx

For our client, an international pharma company in Basel, we are looking for a highly motivated and experienced Technical QA Manager to join a dynamic IMP Quality Systems and Qualification/Validation team.Thr IMP Quality Systems and Qualification/Validation team plays a key role in ensuring GMP compliance of facilities and systems used for the manufacture of Investigational Medicinal Products (IMPs). The team covers production facilities for the chemical

On behalf of one of our clients, we are looking for a Biomarker Clinical Operations Lead in PDG. The person in this role will be responsible and accountable to provide Biomarker operational expertise by planning, coordinating, and overseeing all operational activities for the lifecycle of biomarker and companion diagnostic samples and data, for PDG clinical studies. General Information: Start date: ASAPPlanned duration: unlimited contract via